Trisubstituted Alkenes as Valuable Building Blocks

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F25%3A43933822" target="_blank" >RIV/60461373:22310/25:43933822 - isvavai.cz</a>
Result on the web
<a href="https://www.mdpi.com/1420-3049/30/16/3370" target="_blank" >https://www.mdpi.com/1420-3049/30/16/3370</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3390/molecules30163370" target="_blank" >10.3390/molecules30163370</a>

Result language
angličtina
Original language name
Trisubstituted Alkenes as Valuable Building Blocks
Original language description
The stereoselective synthesis of trisubstituted alkenes has become a key topic in modern organic chemistry. At the same time, trisubstituted alkenes also serve as valuable starting materials for a wide range of transformations. However, it remains unclear to what extent these alkenes are utilized in comparison to their mono- and disubstituted counterparts. This review aims to provide a comprehensive overview of fundamental transformations involving all-carbon-substituted trisubstituted alkenes. The first section focuses on additions of carbon, oxygen, and nitrogen nucleophiles, as well as halogenation and carboxylation reactions. The second part discusses oxidative cleavage processes, while the final section addresses the cyclization and cycloisomerization reactions of trisubstituted alkenes. © 2025 by the authors.
Czech name
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Czech description
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Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10400 - Chemical sciences

Publication year
2025
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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